
501 - 1000 employees
Founded 2000
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Emerald Clinical is a leading global clinical research organization (CRO) founded in the Asia‑Pacific region that provides end‑to‑end clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and post‑marketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.
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501 - 1000 employees
Founded 2000
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Emerald Clinical is a leading global clinical research organization (CRO) founded in the Asia‑Pacific region that provides end‑to‑end clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and post‑marketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.
• Plan and implement the set-up, programming, and ongoing maintenance of data management systems for clinical research projects • Ensure complete, accurate, and high-quality research data for final analysis • Take on project management responsibilities for assigned projects where appropriate • Liaise with Research Fellows, Division Heads, Project Managers, and external parties to determine data collection and reporting requirements • Design or assist in designing electronic data collection systems • Design or assist in designing Case Report Forms and other data collection tools • Maintain data collection systems • Participate in developing and validating new data management systems and processes • Design and generate data reports • Mentor, train, and supervise data management staff • Plan projects and resources • Collaborate with clinical, programming, statistics, and other project team members • Lead or participate in special projects to improve processes, tools, systems, and organization • Complete and attend mandatory training • Participate in objective setting, performance management, role reviews, and career development activities • Participate in project management, organizational meetings, and workshops • Comply with regulations, guidelines, SOPs, project requirements, and relevant systems • Perform quality control and report or escalate risks and issues • Contribute to internal meetings, continuous improvement, knowledge sharing, and staff development • Comply with Work Health and Safety legislation and practices
• Tertiary qualifications in science or related field • 10–12 years of increasing responsibility in data coordination of clinical trials • Strong IT skills, including SQL, reporting software, all Microsoft Office applications, web-based databases, and the Internet • Strong conceptual ability to learn new software applications quickly • Experience with statistical packages desired but not essential • Proven ability to handle large data sets, including reporting and evaluation procedures • Strong understanding of relevant Good Clinical Practice, NHMRC, and TGA regulatory guidelines, especially regarding data quality and accuracy • Ability to evaluate and recommend changes to existing processes and procedures • Excellent time management and project management skills • Excellent written and verbal communication skills • High-level problem-solving, analytical, and strategic thinking skills • Excellent interpersonal skills and ability to work flexibly, autonomously, in small teams, and with varied stakeholders including senior management • Technological proficiency with Microsoft Office packages • Ability to focus on both strategic context and detail/quality • Flexibility and adaptability in changing and ambiguous environments
• Purpose-driven work contributing to clinical trials in renal, cardiometabolic, and oncology therapies • Competitive compensation with a tailored salary and benefits package • Hybrid or remote working arrangements, depending on location and role • Learning opportunities and access to a global network of scientific leaders • Employee wellbeing programs promoting work-life balance, health, and team connection • Global engagement surveys • Recognition programs • Team-building events • Exposure to diverse international projects and clients
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